Yvonne O'Connor

Understanding Mobile Technology Post-Adoption Behaviour: Impact upon Knowledge Creation and Individual Performance

Substantial growth in mobile technologies has revolutionised how individuals within industries conduct their work. However, after significant investments in Information Systems innovations existing evidence strongly suggests that Information Systems are often under-utilised following implementation. Therefore, it is important to understand post adoption behaviour at an infusion phase. Offering real-time information, mobile technologies are transforming how health care services are delivered. Currently, the extent to which post adoption behaviours from using m-health technologies impacts knowledge creation and an individuals performance is under investigated. In order to bridge this gap and extending existing research in the Information Systems field, a conceptual modelis developed to investigate m-health technology post-adoption behavior (i.e. integrative and exploratory use) relating to their impact upon knowledge creation and individual performance.

Privacy by Design: Informed consent and Internet of Things for smart health

Abstract Check: I accept the terms and conditions and privacy policy statements associated with this technological artefact! The informed consent process is becoming more of a challenge with the emergence of Internet of Things (IoT) as data may be collected without the digital health citizen being aware. It is argued in this paper that the first phase for universal usability of IoT within the smart health domain is to ensure that digital health citizens (i.e. user of technology) are fully aware of what they are consenting to when they register an account with such technological artefacts. This point is further reinforced by the proposed ‘Privacy by Design’ requirements associated with the forthcoming General Data Protection Regulation (GDPR). This paper proposes some practical approaches which should be considered when designing and developing IoT for data collection and data sharing within the health domain.

A mobile health technology intervention for addressing the critical public health issue of child mortality

Evaluations of development initiatives in resource‐poor settings dominate Health Information Technology/Systems research. Yet a dearth of research exists, which documents the design and development of these technological artefacts. Through the lens of Transition Management Framework, this research attempts to address this gap in literature, to describe a particular technology (ie, Supporting LIFE—SL eCCM App) and the way in which its hardware, software, and system configurations interact with the sociocultural and economic context in one rural region of the Malawian community. This study uses a design science perspective to ensure the design and development of a health technology intervention that is relevant and has utility in the context for which it has been built, ie, Malawi Africa. This paper addresses the manner in which the configurations of a mobile Health intervention (known as Supporting LIFE eCCM App) interact within a developing world context. Supporting LIFE eCCM aims to leverage the critical societal issue of reducing child mortality in Malawi, Africa. The design science approach supports the design and build of a health intervention that is a good fit for the “real‐world” health scenario considered. Coupled with Geels Transition Management Framework, we emphasise the need for a balanced sociotechnical approach to mHealth, placing individuals at the centre of the IT development project while also considering social, economic, and cultural factors. These are key environmental aspects of a development project such as this one.

Predicting Participant Consent in mHealth Trials – A Caregiver’s Perspective

Informed consent is sought prior to conducting a healthcare intervention on a person. When a healthcare intervention involves a young child, their caregiver is required to provide informed consent on their behalf. However, little is known on the behavioural intentions of participants to provide consent when a mobile health (mHealth) intervention is involved in a clinical trial scenario. Understanding this phenomenon is important, without consent appropriate data may not be collected to empirically examine the implications of mHealth initiatives when delivering healthcare services to children in a ‘real world context’. The objective of this paper is to explore the behavioural intentions of caregivers to provide consent for children (under five years of age) to participate in mHealth Randomised Control Trials (RCT) in developing countries and subsequently develop a predictive model for consent giving. Data was captured vis-a-vis interviews with Malawian caregivers in Africa. The findings reveal that emotional response stimuli play a major role during the participant informed consent process resulting in the involvement (or not) of a child within an RCT. The study contributes to, and opens up, avenues for critical research on the role of informed consent as part of RCT-related projects, especially concerning the involvement of children. This new knowledge may be leveraged to address participant uncertainties and subsequently improve the rate of paediatric recruitment in mHealth trial scenarios.